APA (7th ed.) Citation

Chen, W., & Hu, J. (2025). A heterozygous nonsense mutation in the FGB gene (c.1299G > A) causes congenital fibrinogen disorder across four consecutive generations. Thrombosis Journal, 23(1), 1. https://doi.org/10.1186/s12959-025-00746-4

Chicago Style (17th ed.) Citation

Chen, Wanling, and Jiasheng Hu. "A Heterozygous Nonsense Mutation in the FGB Gene (c.1299G > A) Causes Congenital Fibrinogen Disorder Across Four Consecutive Generations." Thrombosis Journal 23, no. 1 (2025): 1. https://doi.org/10.1186/s12959-025-00746-4.

MLA (9th ed.) Citation

Chen, Wanling, and Jiasheng Hu. "A Heterozygous Nonsense Mutation in the FGB Gene (c.1299G > A) Causes Congenital Fibrinogen Disorder Across Four Consecutive Generations." Thrombosis Journal, vol. 23, no. 1, 2025, p. 1, https://doi.org/10.1186/s12959-025-00746-4.